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反复吗啡处理后关键脑奖励区域中 H19、BC1、MIAT1 和 MALAT1 长非编码 RNA 的差异表达。

Differential expression of H19, BC1, MIAT1, and MALAT1 long non-coding RNAs within key brain reward regions after repeated morphine treatment.

机构信息

Department of Biological Science, Faculty of Science, University of Kurdistan, Sanandaj, Iran.

Department of Biological Science, Faculty of Science, University of Kurdistan, Sanandaj, Iran.

出版信息

Behav Brain Res. 2021 Sep 24;414:113478. doi: 10.1016/j.bbr.2021.113478. Epub 2021 Jul 21.

Abstract

Morphine-induced analgesic tolerance and dependence are significant limits of pain control; however, the exact molecular mechanisms underlying morphine tolerance and dependence have remained unclear. The role of long non-coding RNAs (lncRNAs) in morphine tolerance and dependence is yet to be determined. We aimed to explore the association of specific lncRNAs expression in key brain reward regions after repeated injection of morphine. Male Wistar rats received subcutaneous injections of twice-daily morphine (10 mg/kg) or saline (1 mL/kg) for eight days. On day 8 of the repeated injections, induction of morphine analgesic tolerance and dependence was confirmed through a hotplate test and a naloxone-precipitated withdrawal analysis, respectively. Expression of H19, BC1, MIAT1, and MALAT1 lncRNAs was determined from the midbrain, striatum, hypothalamus, prefrontal cortex (PFC), and hippocampus by real-time PCR on day 8 of the repeated injections. The H19 expression was significantly different between morphine-treated and control saline-treated rats in all investigated areas except for the hippocampus. The BC1 expression significantly altered in the midbrain, hypothalamus, and hippocampus, but not in the striatum and PFC after repeated morphine treatment. The MIAT1 and MALAT1 expression site-specifically altered in the midbrain, hypothalamus, and striatum; however, no significant changes were detected in their expression in the PFC and hippocampus after repeated morphine treatment. We conclude that alterations in the expression of these lncRNAs in the brain reward regions especially in the midbrain, striatum and hypothalamus may have critical roles in the development of morphine dependence and tolerance, which need to be considered in future researches.

摘要

吗啡诱导的镇痛耐受和依赖是疼痛控制的显著限制;然而,吗啡耐受和依赖的确切分子机制仍不清楚。长链非编码 RNA(lncRNA)在吗啡耐受和依赖中的作用尚未确定。我们旨在探讨在重复注射吗啡后关键脑奖励区域中特定 lncRNA 表达的相关性。雄性 Wistar 大鼠接受每日两次皮下注射吗啡(10mg/kg)或生理盐水(1ml/kg),共 8 天。在重复注射的第 8 天,通过热板试验和纳洛酮诱发戒断分析分别确认吗啡镇痛耐受和依赖的诱导。在重复注射的第 8 天,通过实时 PCR 从中脑、纹状体、下丘脑、前额叶皮层(PFC)和海马确定 H19、BC1、MIAT1 和 MALAT1 lncRNA 的表达。除海马体外,吗啡处理大鼠和对照生理盐水处理大鼠的所有研究区域的 H19 表达均有显著差异。BC1 在中脑、下丘脑和海马表达明显改变,但重复吗啡处理后纹状体和 PFC 无明显改变。MIAT1 和 MALAT1 在中脑、下丘脑和纹状体中特异性表达改变,但重复吗啡处理后其在 PFC 和海马中的表达无明显变化。我们得出结论,这些 lncRNA 在脑奖励区域中的表达改变,特别是在中脑、纹状体和下丘脑,可能在吗啡依赖和耐受的发展中具有关键作用,这需要在未来的研究中加以考虑。

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